Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

FIAX TEST KIT FOR TOBRAMYCIN QUANTITA

K-Number: K801308 · 1980-06-20

Decision Date1980-06-20
Product CodeLCR
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

FIAX TEST KIT FOR TOBRAMYCIN QUANTITA is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Diagnostic Technology. It received FDA 510(k) clearance on 1980-06-20 under 510(k) number K801308. The device is classified under product code LCR. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIAX TEST KIT FOR TOBRAMYCIN QUANTITA?

FIAX TEST KIT FOR TOBRAMYCIN QUANTITA is a medical device that received FDA 510(k) clearance on 1980-06-20. The listed applicant is Intl. Diagnostic Technology. The 510(k) number is K801308.

When did FIAX TEST KIT FOR TOBRAMYCIN QUANTITA receive FDA 510(k) clearance?

FIAX TEST KIT FOR TOBRAMYCIN QUANTITA received FDA 510(k) clearance on 1980-06-20, under 510(k) number K801308.

Who is the listed applicant for FIAX TEST KIT FOR TOBRAMYCIN QUANTITA?

The FDA 510(k) record lists Intl. Diagnostic Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIAX TEST KIT FOR TOBRAMYCIN QUANTITA?

The FDA product code for FIAX TEST KIT FOR TOBRAMYCIN QUANTITA is LCR.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Intl. Diagnostic Technology as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 29 devices →

Related Devices (Code: LCR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑